Recent content by Yokoko

  1. Yokoko

    Chemistry Please confirm my Activity Coefficient Calculations

    Oops thanks, I misread your earlier message. With I = 0.0666 I get an overall value of 0.41 which fits. Thanks again!
  2. Yokoko

    Chemistry Please confirm my Activity Coefficient Calculations

    Thanks for your answer. Again, I'm not sure if I understood this correctly. I used c as I thought s = c for simple ions. I now took the root of √I to get I. I assumed the C for KNO3 = 0.0050 and C for CaSO4 = s = 0.0154 This might be where I am wrong?
  3. Yokoko

    Chemistry Predicting the dependence of Solubility on Ionic Strength

    All solved. Would delete but I'm not sure how.
  4. Yokoko

    Chemistry How do I form the product with alkylation and condensation?

    I don't really know how to begin. I've done alkylations by having two of the same compounds react with each other e.g. two aldehydes but never started out with dimethyl malonate. I was thinking I need 1,4 dibromobutane to form the cyclopentane ring but apart from that I'm clueless
  5. Yokoko

    Chemistry Help with mol and volume calculations - Cram's rule

    Apologies, that makes sense! It seems like I put the equation the wrong way around ie calculated 24.305/60.8 instead of 60.8/24.305. So the moles for each of the compounds are 2.5, leaving me with 453.28g of phenyl magnesium bromide The equivalent numbers were probably this wrong because I...
  6. Yokoko

    Chemistry Help with mol and volume calculations - Cram's rule

    I have worked the following out: 72.5g of phenyl magnesium bromide are prepared from the reagents. I tried to take it a step further and create the same table for the reaction of phenyl magnesium bromide and 2-phenyl propanal but I'm unsure whether I can infer it like that - especially given...
  7. Yokoko

    Chemistry Help with mol and volume calculations - Cram's rule

    Am I right to assume that the equivalents for phenyl magnesium bromide would be 3 (magnesium, bromobenzene and ether (?)) And the number for 2-phenyl-propanal 1 as it says "...was added to 2-phenylpropionaldehyde" which is the same thing as 2-phenylpropanal? I don't know if I understood this...
  8. Yokoko

    Chemistry Molecular Orbital for Sn2 reaction

    That makes sense! Thank you so much for help, I know it took a while!
  9. Yokoko

    Chemistry Molecular Orbital for Sn2 reaction

    So, this should be right now. I forgot about the negative charge on the sulfur, I think that was my mistake.
  10. Yokoko

    Chemistry Molecular Orbital for Sn2 reaction

    Oh you are right, the C would be lower in energy, therefore under the SEt orbital. And since the bond with sodium breaks, it seems like it only has an unpaired electron left
  11. Yokoko

    Chemistry Molecular Orbital for Sn2 reaction

    I think I've come a bit farther this time. The bonding/anti bonding hint really helped! :) Two questions: is there only one or two e- in the orbital of SEt- ? It is a lone pair, so there would be 2 e-, correct? And would the orbital diagram drawn enough to answer the question combined with...
  12. Yokoko

    Chemistry Molecular Orbital for Sn2 reaction

    Thanks for your input! I know it's not a lot but I started working upon your prompts. In the first one is the orbital attacking the C centre with the positive charge after Br has left. Maybe it would be good to but Br- on the side too? The second one is my attempt at the orbital diagram...
  13. Yokoko

    Chemistry Molecular Orbital for Sn2 reaction

    The equation can be seen in the picture. I was assuming it was an Sn2 reaction given the polar aprotic solvent and strong nucleophile. For b), I assumed that the question asked me to draw the orbitals as shown above (as opposed to orbital diagram) because it asked me to identify the HOMO and...
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